Canonical Allele Identifier: CA377485667
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs876661234

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960961T>G , CM000672.2:g.87960961T>G GRCh38
NC_000010.10:g.89720718T>G , CM000672.1:g.89720718T>G GRCh37
NC_000010.9:g.89710698T>G NCBI36
NG_007466.2:g.102523T>G , LRG_311:g.102523T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.962T>G ENSP00000514759.2:p.Val321Gly
ENST00000710265.1:c.869T>G ENSP00000518161.1:p.Val290Gly
ENST00000472832.3:c.869T>G ENSP00000483066.2:p.Val290Gly
ENST00000688158.2:n.1604T>G
ENST00000688922.2:c.*699T>G ENSP00000508742.2:n.*699T>G
ENST00000700021.1:c.824T>G ENSP00000514757.1:p.Val275Gly
ENST00000700022.1:c.*208T>G ENSP00000514758.1:n.*208T>G
ENST00000700023.1:n.2027T>G
ENST00000700024.1:n.2261T>G
ENST00000700025.1:n.1638T>G
ENST00000700026.1:n.506T>G
ENST00000700029.1:c.796T>G
ENST00000706954.1:c.869T>G ENSP00000516674.1:p.Val290Gly
ENST00000706955.1:c.*904T>G ENSP00000516675.1:n.*904T>G
ENST00000686459.1:c.*455T>G ENSP00000508909.1:n.*455T>G
ENST00000688158.1:c.*980T>G ENSP00000509254.1:n.*980T>G
ENST00000688308.1:c.869T>G ENSP00000508752.1:p.Val290Gly
ENST00000688922.1:c.790T>G
ENST00000693560.1:c.1388T>G ENSP00000509861.1:p.Val463Gly
ENST00000371953.8:c.869T>G MANE Select ENSP00000361021.3:p.Val290Gly
ENST00000371953.7:c.869T>G ENSP00000361021.3:p.Val290Gly
ENST00000472832.2:c.296T>G ENSP00000483066.1:p.Val99Gly
NM_000314.5:c.869T>G NP_000305.3:p.Val290Gly
NM_000314.6:c.869T>G NP_000305.3:p.Val290Gly
NM_001304717.2:c.1388T>G NP_001291646.2:p.Val463Gly
NM_001304718.1:c.278T>G NP_001291647.1:p.Val93Gly
XM_006717926.2:c.824T>G XP_006717989.1:p.Val275Gly
XM_011539981.1:c.869T>G XP_011538283.1:p.Val290Gly
XM_011539982.1:c.773T>G XP_011538284.1:p.Val258Gly
XR_945791.1:n.1439T>G
NM_000314.7:c.869T>G NP_000305.3:p.Val290Gly
NM_001304717.5:c.1388T>G NP_001291646.4:p.Val463Gly
NM_001304718.2:c.278T>G NP_001291647.1:p.Val93Gly
NM_000314.8:c.869T>G MANE Select NP_000305.3:p.Val290Gly